Search for a gene
SLC26A2 - solute carrier family 26 member 2
- Synonym(s) : DTDST
- Previous symbols and names : 'solute carrier family 26 (sulfate transporter), member 2', DTD, Solute carrier family 26 (sulfate transporter), member 2, solute carrier family 26 (anion exchanger), member 2
- Type : gene with protein product
- Chromosomal location : 5q32
- OMIM: 606718
- HGNC: 10994
- UniProtKB: P50443
- Genatlas: SLC26A2
- GenCC: SLC26A2
- Ensembl: ENSG00000155850
- IUPHAR-DB: 1098
- Reactome: P50443
- LOVD: SLC26A2
Diseases list
- Disease-causing germline mutation(s) in Achondrogenesis type 1B
ORPHA:93298 - Disease-causing germline mutation(s) in Atelosteogenesis type II
ORPHA:56304 - Disease-causing germline mutation(s) in Multiple epiphyseal dysplasia type 4
ORPHA:93307 - Disease-causing germline mutation(s) (loss of function) in Diastrophic dysplasia
ORPHA:628

Additional information
Patient-centred resources for this gene
Research activities on this gene
Specialised Social Services
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.
Orphanet is part of the Gene Curation Coalition, a global effort to harmonise gene-level resources.